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Year : 2017  |  Volume : 18  |  Issue : 1  |  Page : 48-50

Goldmann-Favre syndrome

Department of Ophthalmology, Faculty of Medicine, Alexandria University, Alexandria, Egypt

Correspondence Address:
Moemen S El-Nawawy
15 Mohamed Wagih Ahmed Street, Wabour El-Maya, Alexandria, 21515
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/1110-9173.201617

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Goldmann-Favre syndrome is a rare autosomal recessive vitreoretinal dystrophy that appears usually during childhood, and it manifests with progressive loss of visual acuity, night blindness, and poor color recognition. Fundus findings include degenerative pigmentary changes with macular edema and retinoschisis.

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